Ghent University Academic Bibliography

Your filters: cql: author="VAN BROECKHOVEN, C" or (type any "bookEditor issueEditor" and editor="VAN BROECKHOVEN, C")

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- Conference Paper
- C3
In-depth phenotypic description of TBK1 mutations ; a frequent cause of FTD and ALS in the Flanders-Belgian population

H Gossye, S Van Mossevelde, J Van der Zee, Y Vermeiren, N De Roeck, Jan De Bleecker (UGent) , P Cras, P De Deyn, S Engelborghs, Tim Van Langenhove (UGent) , et al.

(2021) EUROPEAN JOURNAL OF NEUROLOGY. In European Journal of Neurology 28(S1). p.93-94
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- Conference Paper
- C3
Extensive genetic and phenotypic description of MAPT p.R406W in the Flanders-Belgian population

H Gossye, S Van Mossevelde, J Van der Zee, Y Vermeiren, N De Roeck, A Sieben, Jan De Bleecker (UGent) , P De Deyn, P Cras, S Engelborghs, et al.

(2021) EUROPEAN JOURNAL OF NEUROLOGY. In European Journal of Neurology 28(S1). p.94-95
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Contribution of homozygous and compound heterozygous missense mutations in VWA2 to Alzheimer's disease

J Hoogmartens, E Hens, S Engelborghs, R Vandenberghe, PP De Deyn, R Cacace, C Van Broeckhoven, BELNEU Consortium, P. Cras, J. Goeman, et al.

(2021) NEUROBIOLOGY OF AGING. 99. p.100.e9-100.e15
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- Journal Article
- A1
- open access
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD

S Boeynaems, Elke Bogaert (UGent) , E Michiels, I Gijselinck, Anne Sieben, A Jovičić, G De Baets, W Scheveneels, J Steyaert, I Cuijt, et al.

(2016) SCIENTIFIC REPORTS. 6.
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- Journal Article
- A1
- open access
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

I Gijselinck, S Van Mossevelde, J van der Zee, Anne Sieben, S Engelborghs, Jan De Bleecker (UGent) , A Ivanoiu, O Deryck, D Edbauer, M Zhang, et al.

(2016) MOLECULAR PSYCHIATRY. 21(8). p.1112-1124
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Diffusion Kurtosis imaging: a possible MRI biomarker for AD diagnosis?

H Struyfs, W Van Hecke, J Veraart, J Sijbers, S Slaets, Maya De Belder (UGent) , L Wuyts, B Peters, K Sleegers, C Robberecht, et al.

(2015) JOURNAL OF ALZHEIMERS DISEASE. 48(4). p.937-948
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- Journal Article
- A1
Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

J Chapuis, F Hansmannel, M Gistelinck, A Mounier, C Van Cauwenberghe, KV Kolen, F Geller, Y Sottejeau, D Harold, P Dourlen, et al.

(2013) MOLECULAR PSYCHIATRY. 18(11). p.1225-1234
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- Journal Article
- A1
Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis

Elke Bogaert (UGent) , A Goris, P Van Damme, V Geelen, R Lemmens, MA van Es, LH van den Berg, K Sleegers, N Verpoorten, V Timmerman, et al.

(2012) NEUROBIOLOGY OF AGING. 33(2). p.418-420
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- Journal Article
- A1
Glucocorticoid receptor gene-based SNP analysis in patients with recurrent major depression

D Van West, F Van den Eede, J Dem-Fevero, D Souery, KF Norrback, C Van Duijn, C Sluijs, R Adolfsson, R Mendlewicz, Dirk Deboutte (UGent) , et al.

(2006) NEUROPSYCHOPHARMACOLOGY. 31(3). p.620-627
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- Journal Article
- A1
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD

J VAN DER ZEE, R RADEMAKERS, S ENGELBORGHS, I GIJSELINCK, V BOGAERTS, R VANDENBERGHE, Patrick Santens (UGent) , J CAEKEBEKE, T DE POOTER, K PEETERS, et al.

(2006) BRAIN. 129. p.841-852

Academic Bibliography

In-depth phenotypic description of TBK1 mutations ; a frequent cause of FTD and ALS in the Flanders-Belgian population

Extensive genetic and phenotypic description of MAPT p.R406W in the Flanders-Belgian population

Contribution of homozygous and compound heterozygous missense mutations in VWA2 to Alzheimer's disease

Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD

The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

Diffusion Kurtosis imaging: a possible MRI biomarker for AD diagnosis?

Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis

Glucocorticoid receptor gene-based SNP analysis in patients with recurrent major depression

A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD

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